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Life's a Polyp Foundation - Familial Adenomatous Polyposis (FAP) Support
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Jenny’s Personal Blog Library

  • Life's a Polyp Foundation – Familial Adenomatous Polyposis (FAP) Support
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  • Blog
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Year Published

Year Published
  • 2025 (2)
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  • 2012 (24)

Ostomy Reversal Anniversary – 20 Years

20th Anniversary of My Ostomy Reversal

The Evolution of Myself with Chronic Illness

My Journey to Self-Acceptance with Chronic Illness

How Reiki Affected My Mental Health

Unintentionally Using Reiki for Self Care

Vertigo and Physical Therapy

Utilizing Physical Therapy to Decrease Nausea

Understanding Dehydration

Dehydration Issues without a Colon

Continent Ileostomies

Another Kind of Ostomy: The Continent Ileostomy

Accepting Body Changes

Learning Self-Image Esteem

Socializing in a Pandemic

A Look Back on this Year with Covid

FAP and a Feeding Tube: Jeni LeeAnn’s Story

Jeni LeeAnn Shares about Life with Familial Adenomatous Polyposis and a Feeding Tube

Navigating and Understanding School Accommodations

Seeking School Accommodations – 504s and IEPs

Vacationing Amidst a Global Pandemic with Chronic Illness

Celebrating a New Relationship Amidst a Global Pandemic and Chronic Illness

Sensory Deprivation Tanks

Experiencing a Sensory Deprivation Float Tank

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Yukon, OK 73085

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This content is not intended as a substitute for professional medical advice, diagnosis, or treatment. Should you require medical advice, please contact a qualified medical professional who is familiar with FAP.

The Life’s a Polyp Foundation is recognized by the IRS as a 501(c)(3) organization, and donations are tax deductible to the full extent allowed by law. EIN: 41-2433114

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